Health Condition 1: R652- Severe sepsis
Conditions
Interventions
Intervention1: Adding oral midodrine to intervention group: Adding Oral or through Ryles tube of midodrine tablet of 10 mg QID to intervention group till patient is become off from inotrope support
Sponsors
None listed
Eligibility
Inclusion criteria
Inclusion criteria: Septic shock patients on dual vasopressor support
Exclusion criteria
Exclusion criteria: CKD PREGNANCY PRE-EXISTING LOVER DISEASE BRADYCARDIA of Severe organic heart disease Known allergy to midodrine
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time is taken to de-escalate to a single low-dose vasopressor (defined as noradrenaline =0.15 µg/kg/min) after administration of oral midodrine or placebo.Timepoint: During the course of icu stay | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Vasoactive inotropic score (VIS) score trend, recorded 6th hourly till the patient is off inotropic support. Timepoint: During the icu stay;2. Maximum VIS score during ICU stay. Timepoint: During the icy stay;3. Mean VIS during ICU stay. Timepoint: During icu stay;4. Time taken for complete weaning off from inotropic support (in hours). Timepoint: During the Icu stay;5. Length of ICU stay. Timepoint: During the Icu stay;6. Mortality during ICU stay,Timepoint: During the Icu stay | — |
Countries
India
Contacts
Public ContactDr ANAS V P
PGIMER CHANDIGARH
Outcome results
None listed